Oxipurinol
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Preferred IUPAC name 1H-pyrazolo[3,4-d]pyrimidine-4,6(2H,5H)-dione | |
Other names 2,5-Dihydro-1H-pyrazolo[3,4-d]pyrimidine-4,6-dione Alloxanthine | |
Identifiers | |
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3D model (JSmol) |
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Beilstein Reference | 139956 |
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ECHA InfoCard | 100.017.792 |
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MeSH | Oxypurinol |
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InChI
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Properties | |
Chemical formula | C5H4N4O2 |
Molar mass | 152.11086 |
Appearance | white crystals |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references |
Chemical compound
Oxipurinol (INN, or oxypurinol USAN) is an inhibitor of xanthine oxidase.[1] It is an active metabolite of allopurinol and it is cleared renally.[2] In cases of renal disease, this metabolite will accumulate to toxic levels. By inhibiting xanthine oxidase, it reduces uric acid production. High serum uric acid levels may result in gout, kidney stones, and other medical conditions.
References
- ^ Stocker, Sophie L; McLachlan, Andrew J; Savic, Radojka M; Kirkpatrick, Carl M; Graham, Garry G; Williams, Kenneth M; Day, Richard O (2012). "The pharmacokinetics of oxypurinol in people with gout". British Journal of Clinical Pharmacology. 74 (3): 477–489. doi:10.1111/j.1365-2125.2012.04207.x. PMC 3477349. PMID 22300439.
- ^ Elion, Gertrude B; Yü, Ts'ai-Fan; Gutman, Alexander B; Hitchings, George H (1968). "Renal clearance of oxipurinol, the chief metabolite of allopurinol". The American Journal of Medicine. 45 (1): 69–77. doi:10.1016/0002-9343(68)90008-9. PMID 5658870.
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(ligands)
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(blockers)
CNTsTooltip Concentrative nucleoside transporters |
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ENTsTooltip Equilibrative nucleoside transporters | |
PMATTooltip Plasma membrane monoamine transporter |
(inhibitors)
XOTooltip Xanthine oxidase | |
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Others |
See also: Receptor/signaling modulators
This article about a heterocyclic compound is a stub. You can help Wikipedia by expanding it. |
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